A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145999



Internal ID345204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:69944350..69956682hg38UCSC Ensembl
chr16:69978253..69990585hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3812333
hg1912333
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17707155
Samples
Known GenesCLEC18A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145999
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer